Deviation Management, Written Reports, Avoiding Budget Collapse Among Session Topics
For the first time ever, Q1 Productions will host the Medical Device Verification and Validation Conference in Alexandria, Virginia, offering attendees an all-encompassing process and software V&V meeting with high-level session topics and a multitude of networking opportunities. The conference will be held July 24-25, 2014.
The conference provides attendees with two days chock-full of top-of-mind discussion topics, interactive panels and hands-on workshops with fellow verification and validation engineers and professionals. Topics to be addressed include deviation management, understanding QSIT expectations, obstacles of offshoring, scope of validation in written reports, and best practices in documentation. Several "top 40" companies within the medical device and diagnostic industries will lead sessions at the conference, including Johnson & Johnson, Stryker, Baxter International, Covidien, and Medtronic.
This program will create an opportunity for networking and knowledge share amongst participants with engaging and high-level presentations, drawing upon years of experience in the medical device and diagnostic field. Hand-on workshop activities will provide attendees with an opportunity to initiate mock-audit scenarios, providing not only practical knowledge, but also real-time feedback from peers and conference presenters. Dual tracks considering both process validation and software validation cover the full spectrum of medical device verification and validation, making this conference the only one of its kind.
For more information or to register for the Medical Device and Diagnostic Verification and Validation Conference, or on any of Q1 Productions' conferences, please visit www.q1productions.com. Follow the conference on Twitter, @Q1Productions, #q1ddvv.
About the Organizer
Q1 Productions designs and develops webinars, training courses, conference programs and forums aimed at specifically targeted audiences throughout highly regulated industries in order to provide strategic learning and timely program content. Through a highly structured production process focused on research calls with end-users and key stakeholders in the industry, our team is able to understand the immediate business concerns of today's leading executives. Whether focusing on new or pending legislative and health policy issues or enhanced technologies or processes that will drive efficiency, our programs provide solutions to the urgent educational and information needs of our attendees.